Aortic intimal sarcomas are rare among the already uncommon primary aortic neoplasms. Due to a low index of suspicion, characteristic radiographic and clinical findings are sometimes misattributed and the diagnosis is not made until autopsy. We describe the helical CT findings of a patient with an advanced aortic intimal sarcoma, intraluminal and extraluminal disease, and extensive metastases.
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http://dx.doi.org/10.1097/00005382-200404000-00012 | DOI Listing |
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